Variant report

Variant	nsv10126
Chromosome Location	chr2:112036796-112374762
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3991)
CpG islands
(count:305)
Chromatin interactive
region (count:10)
LncRNA
region (count:80)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:3991 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112165582-112165606	K562	blood:	n/a	n/a
2	ARID3A	chr2:112077982-112078035	K562	blood:	n/a	n/a
3	ARID3A	chr2:112134733-112134923	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:112142989-112143245	K562	blood:	n/a	n/a
5	ARID3A	chr2:112191601-112191749	K562	blood:	n/a	n/a
6	ARID3A	chr2:112221794-112221988	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:112286629-112286892	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:112078700-112078866	K562	blood:	n/a	n/a
9	ARID3A	chr2:112279969-112280556	HepG2	liver:	n/a	n/a
10	ATF1	chr2:112123600-112123901	K562	blood:	n/a	n/a
11	ATF1	chr2:112251003-112251203	K562	blood:	n/a	n/a
12	ATF1	chr2:112139588-112139732	K562	blood:	n/a	n/a
13	ATF1	chr2:112191568-112191846	K562	blood:	n/a	n/a
14	ATF1	chr2:112252616-112252812	K562	blood:	n/a	n/a
15	ATF1	chr2:112174026-112174226	K562	blood:	n/a	n/a
16	ATF1	chr2:112104247-112104437	K562	blood:	n/a	n/a
17	ATF1	chr2:112174751-112174909	K562	blood:	n/a	n/a
18	ATF1	chr2:112165410-112165614	K562	blood:	n/a	n/a
19	ATF2	chr2:112183348-112183699	GM12878	blood:	n/a	n/a
20	ATF2	chr2:112183361-112183645	GM12878	blood:	n/a	n/a
21	ATF2	chr2:112236677-112236938	GM12878	blood:	n/a	n/a
22	ATF3	chr2:112292952-112293475	HepG2	liver:	n/a	chr2:112293252-112293272 chr2:112293263-112293272
23	BACH1	chr2:112143146-112143417	K562	blood:	n/a	n/a
24	BACH1	chr2:112078561-112079019	H1-hESC	embryonic stem cell:	n/a	chr2:112078792-112078806
25	BACH1	chr2:112078641-112078944	K562	blood:	n/a	chr2:112078792-112078806
26	BACH1	chr2:112251425-112251440	K562	blood:	n/a	n/a
27	BATF	chr2:112074557-112074916	GM12878	blood:	n/a	chr2:112074773-112074784
28	BATF	chr2:112240605-112241034	GM12878	blood:	n/a	chr2:112240788-112240798
29	BATF	chr2:112182205-112182825	GM12878	blood:	n/a	n/a
30	BATF	chr2:112195786-112196106	GM12878	blood:	n/a	n/a
31	BATF	chr2:112327815-112328182	GM12878	blood:	n/a	n/a
32	BATF	chr2:112037291-112037501	GM12878	blood:	n/a	n/a
33	BATF	chr2:112248667-112249139	GM12878	blood:	n/a	n/a
34	BATF	chr2:112182048-112182971	GM12878	blood:	n/a	n/a
35	BATF	chr2:112077128-112077551	GM12878	blood:	n/a	n/a
36	BATF	chr2:112158868-112159229	GM12878	blood:	n/a	chr2:112159209-112159219
37	BATF	chr2:112267135-112267389	GM12878	blood:	n/a	n/a
38	BATF	chr2:112072875-112073150	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
39	BATF	chr2:112290692-112291073	GM12878	blood:	n/a	chr2:112290906-112290916 chr2:112290905-112290916
40	BATF	chr2:112303348-112304091	GM12878	blood:	n/a	chr2:112303735-112303744
41	BATF	chr2:112206432-112206650	GM12878	blood:	n/a	n/a
42	BATF	chr2:112250737-112250940	GM12878	blood:	n/a	n/a
43	BATF	chr2:112077193-112077517	GM12878	blood:	n/a	n/a
44	BATF	chr2:112188889-112189327	GM12878	blood:	n/a	n/a
45	BATF	chr2:112250963-112251779	GM12878	blood:	n/a	chr2:112251535-112251545 chr2:112251573-112251582
46	BATF	chr2:112236417-112237152	GM12878	blood:	n/a	n/a
47	BATF	chr2:112195246-112195683	GM12878	blood:	n/a	chr2:112195574-112195583
48	BATF	chr2:112074635-112074933	GM12878	blood:	n/a	chr2:112074773-112074784
49	BATF	chr2:112188947-112189209	GM12878	blood:	n/a	n/a
50	BATF	chr2:112248607-112249357	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112124118-112124168	MCF10A-Er-Src	breast:	n/a
2	chr2:112280286-112280336	IMR90	lung:	fetal
3	chr2:112252254-112252304	CMK	blood:	n/a
4	chr2:112280286-112280336	GM12878	blood:	n/a
5	chr2:112124380-112124430	NHBE	bronchial:	n/a
6	chr2:112252254-112252304	GM12892	blood:	n/a
7	chr2:112124380-112124430	RPTEC	kidney:	n/a
8	chr2:112293267-112293317	HRPEpiC	eye:	n/a
9	chr2:112293267-112293317	BE2_C	brain:	n/a
10	chr2:112124118-112124168	GM12891	blood:	n/a
11	chr2:112124118-112124168	LNCaP	prostate:	n/a
12	chr2:112280286-112280336	H1-hESC	embryonic stem cell:	embryo
13	chr2:112252254-112252304	NHBE	bronchial:	n/a
14	chr2:112252254-112252304	AG04450	lung:	fetal
15	chr2:112280286-112280336	NB4	blood:	n/a
16	chr2:112252254-112252304	HIPEpiC	eye:	n/a
17	chr2:112124118-112124168	HCPEpiC	choroid plexus:	n/a
18	chr2:112252254-112252304	SAEC	small airway:	n/a
19	chr2:112124380-112124430	H1-hESC	embryonic stem cell:	embryo
20	chr2:112280286-112280336	RPTEC	kidney:	n/a
21	chr2:112293267-112293317	SK-N-SH_RA	brain:	n/a
22	chr2:112293267-112293317	BJ	skin:	n/a
23	chr2:112280286-112280336	LNCaP	prostate:	n/a
24	chr2:112124380-112124430	SK-N-SH	brain:	n/a
25	chr2:112252254-112252304	IMR90	lung:	fetal
26	chr2:112124118-112124168	ProgFib	skin:	n/a
27	chr2:112124118-112124168	U87	brain:	n/a
28	chr2:112124380-112124430	HRPEpiC	eye:	n/a
29	chr2:112124380-112124430	NHDF-neo	bronchial:	n/a
30	chr2:112124380-112124430	PANC-1	pancreas:	n/a
31	chr2:112280286-112280336	T-47D	breast:	n/a
32	chr2:112124380-112124430	NT2-D1	testis:	n/a
33	chr2:112280286-112280336	AG10803	skin:	n/a
34	chr2:112124380-112124430	HNPCEpiC	eye:	n/a
35	chr2:112124380-112124430	HPAEpiC	pulmonary alveolar:	n/a
36	chr2:112293267-112293317	IMR90	lung:	fetal
37	chr2:112280286-112280336	MCF-7	breast:	n/a
38	chr2:112280286-112280336	HEEpiC	esophagus:	n/a
39	chr2:112293267-112293317	A549	lung:	n/a
40	chr2:112293267-112293317	HRE	kidney:	n/a
41	chr2:112252254-112252304	HEEpiC	esophagus:	n/a
42	chr2:112293267-112293317	ProgFib	skin:	n/a
43	chr2:112252254-112252304	PFSK-1	brain:	n/a
44	chr2:112124118-112124168	HMEC	breast:	n/a
45	chr2:112252254-112252304	PrEC	prostate:	n/a
46	chr2:112124380-112124430	A549	lung:	n/a
47	chr2:112124118-112124168	AG04449	skin:	fetal
48	chr2:112280286-112280336	HAEpiC	amniotic membrane:	n/a
49	chr2:112124118-112124168	PFSK-1	brain:	n/a
50	chr2:112293267-112293317	GM19239	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:112374742..112377562-chr2:112458693..112461036,2	MCF-7	breast:
2	chr2:112374024..112376697-chr2:112377578..112380485,2	K562	blood:
3	chr2:112158086..112161064-chr8:43095226..43096729,2	MCF-7	breast:
4	chr2:111879395..111881005-chr2:112073345..112075122,2	MCF-7	breast:
5	chr2:111878764..111880387-chr2:112231090..112233888,2	MCF-7	breast:
6	chr2:112239413..112241217-chr2:112461159..112463413,2	MCF-7	breast:
7	chr2:111877393..111879713-chr2:112235053..112237981,2	K562	blood:
8	chr2:111878316..111879893-chr2:112101721..112103928,2	MCF-7	breast:
9	chr2:111877705..111880008-chr2:112211679..112213711,2	MCF-7	breast:
10	chr2:112374717..112376877-chr2:112415569..112417178,2	MCF-7	breast:

(count:80 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BCL2L11-5	chr2:112081840-112081972	l_1923_chr2:112081839-112086268_testes
2	lnc-AC108463.1-3	chr2:112125064-112125152	NONHSAT073622
3	lnc-AC108463.1-3	chr2:112108185-112108338	ENSG00000172965.6
4	lnc-AC108463.1-3	chr2:112227364-112227376	NONHSAT073639
5	lnc-BCL2L11-3	chr2:112257365-112258585	NONHSAT073656
6	lnc-AC108463.1-3	chr2:112101668-112101814	ENSG00000172965.6
7	lnc-AC108463.1-6	chr2:112053206-112053623	NONHSAT073635
8	lnc-BCL2L11-3	chr2:112249107-112249838	NONHSAT073656
9	lnc-MERTK-1	chr2:112365418-112365592	XLOC_001626
10	lnc-AC108463.1-3	chr2:112252462-112252625	ENSG00000172965.6
11	lnc-AC108463.1-3	chr2:112252462-112252611	ENSG00000172965.6
12	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
13	lnc-BCL2L11-3	chr2:112257365-112258585	NONHSAT073658
14	lnc-AC108463.1-3	chr2:112101638-112101675	ENSG00000172965.10
15	lnc-BCL2L11-6	chr2:112060981-112061323	NONHSAT073618
16	lnc-AC108463.1-3	chr2:112252462-112252602	ENSG00000172965.6
17	lnc-AC108463.1-3	chr2:112237746-112237838	ENSG00000172965.6
18	lnc-AC108463.1-3	chr2:112237484-112237657	NONHSAT073639
19	lnc-AC108463.1-3	chr2:112252462-112252631	ENSG00000172965.6
20	lnc-AC108463.1-3	chr2:112227180-112227564	ENSG00000172965.6
21	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
22	lnc-AC108463.1-3	chr2:112071889-112072139	ENSG00000172965.6
23	lnc-BCL2L11-7	chr2:112141329-112142569	NONHSAT073641
24	lnc-AC108463.1-3	chr2:112237484-112237638	ENSG00000172965.6
25	lnc-AC108463.1-3	chr2:112186886-112187197	NONHSAT073642
26	lnc-AC108463.1-3	chr2:112252462-112252610	ENSG00000172965.6
27	lnc-AC108463.1-3	chr2:112125088-112125152	NONHSAT073639
28	lnc-AC108463.1-3	chr2:112252462-112252597	ENSG00000172965.6
29	lnc-AC108463.1-3	chr2:112229566-112229674	ENSG00000172965.6
30	lnc-BCL2L11-5	chr2:112081889-112082063	NONHSAT073637
31	lnc-AC108463.1-3	chr2:112187020-112187197	ENSG00000172965.6
32	lnc-AC108463.1-3	chr2:112227215-112227564	ENSG00000172965.6
33	lnc-AC108463.1-3	chr2:112252462-112252692	NONHSAT073642
34	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.10
35	lnc-AC108463.1-3	chr2:112252462-112252540	NONHSAT073639
36	lnc-AC108463.1-3	chr2:112227095-112227564	ENSG00000172965.6
37	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
38	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
39	lnc-BCL2L11-2	chr2:112037444-112037486	XLOC_001624
40	lnc-MERTK-1	chr2:112369479-112369982	NONHSAT073660
41	lnc-AC108463.1-3	chr2:112252462-112252677	ENSG00000172965.6
42	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
43	lnc-AC108463.1-3	chr2:112237484-112237638	ENSG00000172965.6
44	lnc-BCL2L11-5	chr2:112085950-112086268	l_1923_chr2:112081839-112086268_testes
45	lnc-AC108463.1-2	chr2:112249520-112250145	ENSG00000224959
46	lnc-BCL2L11-3	chr2:112248850-112249239	XLOC_001625
47	lnc-BCL2L11-3	chr2:112268201-112268567	XLOC_001625
48	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
49	lnc-AC108463.1-2	chr2:112252134-112252388	ENSG00000224959
50	lnc-BCL2L11-2	chr2:112043757-112044842	XLOC_001624

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4435	chr2:112078638-112078659	MIMAT0018951_1

No data

Variant related genes	Relation type
ENSG00000240350	TF binding region
ENSG00000224959	TF binding region
ENSG00000225744	TF binding region
RPS14P4	TF binding region
MIR4435-1HG	TF binding region
ENSG00000271635	TF binding region
ENSG00000223973	TF binding region
MIR4435-1	TF binding region
ENSG00000240350	CpG island
ENSG00000224959	CpG island
ENSG00000225744	CpG island
RPS14P4	CpG island
MIR4435-1HG	CpG island
ENSG00000271635	CpG island
ENSG00000223973	CpG island
MIR4435-1	CpG island
ENSG00000153094	chromatin interactions
KLHL24	miRNA target sites
ITSN2	miRNA target sites
ASCC3	miRNA target sites

Extended variants
information (count: 8264 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:8264 , 50 per page) page: 1 2 3 4 5 6 7 ... 166

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533491762	chr2:112036807-112036808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182755532	chr2:112036849-112036850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566891688	chr2:112036856-112036857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs871638	chr2:112036877-112036878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535916082	chr2:112036893-112036894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113648353	chr2:112036895-112036896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568115803	chr2:112036899-112036900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537247362	chr2:112036937-112036938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556916706	chr2:112036938-112036939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544735440	chr2:112036981-112036982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369560554	chr2:112037028-112037029	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs545715298	chr2:112037112-112037113	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs552517788	chr2:112037120-112037121	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs535199799	chr2:112037285-112037286	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs572515173	chr2:112037308-112037309	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs146150535	chr2:112037360-112037361	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs541477939	chr2:112037491-112037492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561820694	chr2:112037526-112037527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530563645	chr2:112037569-112037570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs202222568	chr2:112037586-112037587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544777724	chr2:112037617-112037618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1706155	chr2:112037645-112037646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564554830	chr2:112037650-112037651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533637678	chr2:112037757-112037758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148564326	chr2:112037763-112037764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145420722	chr2:112037819-112037820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547331420	chr2:112037869-112037870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566828432	chr2:112037904-112037905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2176697	chr2:112037967-112037968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1715156	chr2:112038022-112038023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549445514	chr2:112038028-112038029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112401593	chr2:112038066-112038067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544204259	chr2:112038187-112038188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140699396	chr2:112038206-112038207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62161561	chr2:112038209-112038210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550728990	chr2:112038244-112038245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113275577	chr2:112038247-112038248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1706153	chr2:112038447-112038448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1715154	chr2:112038719-112038720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs367875263	chr2:112038828-112038829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552851063	chr2:112038829-112038830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572848880	chr2:112038864-112038865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535075783	chr2:112038882-112038883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546819848	chr2:112038900-112038901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575278585	chr2:112038927-112038928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543993025	chr2:112038950-112038951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564666971	chr2:112039174-112039175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs578222385	chr2:112039185-112039186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540879718	chr2:112039188-112039189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs62161563	chr2:112040072-112040073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Breast cancer	22314128	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:2895 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112008600-112048600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr2:112020600-112048000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:112023400-112046400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:112025600-112116600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr2:112025800-112037800	Weak transcription	HSMM	muscle
6	chr2:112044400-112046600	Weak transcription	Pancreas	Pancrea
7	chr2:112045400-112045600	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr2:112045400-112045800	Enhancers	NHEK	skin
9	chr2:112045400-112046000	Enhancers	HMEC	breast
10	chr2:112045600-112046200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr2:112045800-112047600	Weak transcription	NHEK	skin
12	chr2:112046000-112046400	Weak transcription	HMEC	breast
13	chr2:112046200-112046400	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr2:112046400-112046600	Enhancers	HMEC	breast
15	chr2:112046400-112046800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr2:112046400-112047000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr2:112046400-112047800	Enhancers	Placenta	Placenta
18	chr2:112046400-112048600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr2:112046400-112057400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr2:112046600-112047800	Weak transcription	HMEC	breast
21	chr2:112047000-112047400	Enhancers	Placenta Amnion	Placenta Amnion
22	chr2:112047000-112048400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr2:112047600-112047800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:112047600-112048800	Enhancers	NHEK	skin
25	chr2:112047800-112048600	Weak transcription	Placenta	Placenta
26	chr2:112047800-112049600	Enhancers	HMEC	breast
27	chr2:112047800-112052400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr2:112048000-112048800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr2:112048400-112048600	Enhancers	Pancreas	Pancrea
30	chr2:112048400-112048800	Enhancers	Liver	Liver
31	chr2:112048400-112049000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr2:112048600-112048800	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr2:112048600-112048800	Enhancers	Placenta	Placenta
34	chr2:112048600-112049400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr2:112048600-112049600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr2:112048600-112051000	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr2:112048800-112049200	Weak transcription	Liver	Liver
38	chr2:112048800-112049400	Weak transcription	Placenta	Placenta
39	chr2:112048800-112049600	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr2:112048800-112049800	Enhancers	HSMMtube	muscle
41	chr2:112048800-112069600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr2:112049000-112050600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr2:112049200-112049800	Enhancers	Liver	Liver
44	chr2:112049400-112049600	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr2:112049400-112049600	Enhancers	Placenta	Placenta
46	chr2:112049400-112050000	Weak transcription	K562	blood
47	chr2:112049400-112050200	Enhancers	Fetal Intestine Small	intestine
48	chr2:112049400-112051000	Enhancers	HepG2	liver
49	chr2:112049600-112050800	Weak transcription	Placenta	Placenta
50	chr2:112049800-112050200	Enhancers	Stomach Mucosa	stomach

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